Canonical Allele Identifier: CA2841966366
Gene: KCNJ5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128911907dup , CM000673.2:g.128911907dup GRCh38
NC_000011.9:g.128781802dup , CM000673.1:g.128781802dup GRCh37
NC_000011.8:g.128287012dup NCBI36
NG_023406.2:g.25490dup , LRG_333:g.25490dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.634dup MANE Select ENSP00000433295.1:p.Asp212GlyfsTer?
ENST00000338350.4:c.634dup ENSP00000339960.4:p.Asp212GlyfsTer?
ENST00000529694.5:c.634dup ENSP00000433295.1:p.Asp212GlyfsTer?
ENST00000533599.1:c.634dup ENSP00000434266.1:p.Asp212GlyfsTer?
NM_000890.3:c.634dup , LRG_333t1:c.634dup NP_000881.3:p.Asp212GlyfsTer?
XM_011542809.1:c.634dup XP_011541111.1:p.Asp212GlyfsTer?
XM_011542810.1:c.634dup XP_011541112.1:p.Asp212GlyfsTer?
NM_000890.4:c.634dup NP_000881.3:p.Asp212GlyfsTer?
NM_001354169.1:c.634dup NP_001341098.1:p.Asp212GlyfsTer?
XM_011542809.2:c.634dup XP_011541111.1:p.Asp212GlyfsTer?
XM_011542810.3:c.634dup XP_011541112.1:p.Asp212GlyfsTer?
NM_000890.5:c.634dup MANE Select NP_000881.3:p.Asp212GlyfsTer?
NM_001354169.2:c.634dup NP_001341098.1:p.Asp212GlyfsTer?